A Genocentric Approach to Discovery of Mendelian DisordersHansen, Adam W.; Murugan, Mullai; Li, He; Khayat, Michael M.; Wang, Liwen; Rosenfeld, Jill; Andrews, B. Kim; Jhangiani, Shalini N.; Coban Akdemir, Zeynep H.; Sedlazeck, Fritz J.; Ashley-Koch, Allison E.; Liu, Pengfei; Muzny, Donna M.; Davis, Erica E.; Katsanis, Nicholas; Sabo, Aniko; Posey, Jennifer E.; Yang, Yaping; Wangler, Michael F.; Eng, Christine M.; Sutton, V. Reid; Lupski, James R.; Boerwinkle, Eric; Gibbs, Richard A.; Allori, Alexander; Angrist, Misha; Ashley, Patricia; Bidegain, Margarita; Boyd, Brita; Chambers, Eileen; Cope, Heidi; Cotten, C. Michael; Curington, Theresa; Davis, Erica E.; Ellestad, Sarah; Fisher, Kimberley; French, Amanda; Gallentine, William; Goldberg, Ronald; Hill, Kevin; Kansagra, Sujay; Katsanis, Nicholas; Katsanis, Sara; Kurtzberg, Joanne; Marcus, Jeffrey; McDonald, Marie; Mikati, Mohammed; Miller, Stephen; Murtha, Amy; Perilla, Yezmin; Pizoli, Carolyn; Purves, Todd; Ross, Sherry; Sadeghpour, Azita; Smith, Edward; Wiener, John · The American Journal of Human Genetics · 2019

Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome that Expands the Phenotypic Spectrum of CondensinopathiesKhan, Tahir N.; Khan, Kamal; Sadeghpour, Azita; Reynolds, Hannah; Perilla, Yezmin; McDonald, Marie T.; Gallentine, William B.; Baig, Shahid M.; Davis, Erica E.; Katsanis, Nicholas; Allori, Alexander; Angrist, Misha; Ashley, Patricia; Bidegain, Margarita; Boyd, Brita; Chambers, Eileen; Cope, Heidi; Cotten, C. Michael; Curington, Theresa; Davis, Erica E.; Ellestad, Sarah; Fisher, Kimberley; French, Amanda; Gallentine, William; Goldberg, Ronald; Hill, Kevin; Kansagra, Sujay; Katsanis, Nicholas; Katsanis, Sara; Kurtzberg, Joanne; Marcus, Jeffrey; McDonald, Marie; Mikati, Mohammed; Miller, Stephen; Murtha, Amy; Perilla, Yezmin; Pizoli, Carolyn; Purves, Todd; Ross, Sherry; Sadeghpour, Azita; Smith, Edward; Wiener, John · The American Journal of Human Genetics · 2019

Dissecting Intraflagellar Transport, One Molecule at a TimeDavis, Erica E.; Katsanis, Nicholas · Developmental Cell · 2014

Unique among ciliopathies: primary ciliary dyskinesia, a motile cilia disorderPraveen, Kavita; Davis, Erica E.; Katsanis, Nicholas · F1000Prime Reports · 2015

Interpreting human genetic variation with in vivo zebrafish assaysDavis, Erica E.; Frangakis, Stephan; Katsanis, Nicholas · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2014

The complexity of the cilium: spatiotemporal diversityof an ancient organelleHeydeck, Westley; Fievet, Lorraine; Davis, Erica E; Katsanis, Nicholas · Current Opinion in Cell Biology · 2018

Identification of cis-suppression of human disease mutations by comparative genomicsJordan, Daniel M.; Frangakis, Stephan G.; Golzio, Christelle; Cassa, Christopher A.; Kurtzberg, Joanne; Davis, Erica E.; Sunyaev, Shamil R.; Katsanis, Nicholas · Nature · 2015